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Items: 1 to 20 of 240

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5934711copy number variation1nstd209human GRCh38 chr16: 71,893,011-71,893,306 , GRCh37.p13 chr16: 71,926,914-71,927,209 IST1
    nsv5867643copy number variation1nstd209human GRCh38 chr16: 71,892,813-71,929,297 , GRCh37.p13 chr16: 71,926,716-71,963,200 IST1, PKD1L3
    nsv5711858mobile element insertion1nstd211human GRCh38 chr16: 71,931,418-71,931,418 , GRCh37.p13 chr16: 71,965,321-71,965,321 PKD1L3, IST1
    nsv5669930inversion1nstd207human GRCh38 chr16: 70,123,796-74,346,113 , GRCh37.p13 chr16: 70,157,699-74,380,011 , AARS1, 83 more genes
    nsv5668311inversion1nstd207human GRCh38 chr16: 71,928,859-71,958,785 , GRCh37.p13 chr16: 71,962,762-71,992,684 IST1, PKD1L3
    nsv5557110sequence alteration1nstd206human GRCh38 chr16: 70,117,371-74,396,141 , GRCh37.p13 chr16: 70,151,274-74,430,039 , TAT, 84 more genes
    nsv5517078copy number variation1nstd206human GRCh38 chr16: 71,931,179-71,957,544 , GRCh37.p13 chr16: 71,965,082-71,991,443 IST1, PKD1L3
    nsv5302290copy number variation1nstd204human GRCh38.p13 chr16: 71,905,264-71,906,219 , GRCh37.p13 chr16: 71,939,167-71,940,122 IST1
    nsv5302205copy number variation1nstd204human GRCh38.p13 chr16: 71,925,999-71,926,708 , GRCh37.p13 chr16: 71,959,902-71,960,611 IST1
    nsv5301013copy number variation1nstd204human GRCh38.p13 chr16: 71,923,318-71,923,783 , GRCh37.p13 chr16: 71,957,221-71,957,686 IST1
    nsv5299591copy number variation1nstd204human GRCh38.p13 chr16: 71,904,561-71,909,310 , GRCh37.p13 chr16: 71,938,464-71,943,213 IST1
    nsv5187278mobile element insertion1nstd203human GRCh38 chr16: 71,931,028-71,931,041 , GRCh37.p13 chr16: 71,964,931-71,964,944 IST1, PKD1L3
    nsv5159513mobile element insertion1nstd203human GRCh38 chr16: 71,917,321-71,917,337 , GRCh37.p13 chr16: 71,951,224-71,951,240 IST1
    nsv5151631mobile element insertion1nstd203human GRCh38 chr16: 71,893,018-71,893,047 , GRCh37.p13 chr16: 71,926,921-71,926,950 IST1
    nsv5147845mobile element insertion1nstd203human GRCh38 chr16: 71,893,025-71,893,032 , GRCh37.p13 chr16: 71,926,928-71,926,935 IST1
    nsv5143654mobile element insertion1nstd203human GRCh38 chr16: 71,892,902-71,892,914 , GRCh37.p13 chr16: 71,926,805-71,926,817 IST1
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv4993303copy number variation1nstd200human GRCh38 chr16: 71,931,179-71,957,544 , GRCh37.p13 chr16: 71,965,082-71,991,443 IST1, PKD1L3
    nsv4993302copy number variation1nstd200human GRCh38 chr16: 71,926,007-71,926,699 , GRCh37.p13 chr16: 71,959,910-71,960,602 IST1
    nsv4993301copy number variation1nstd200human GRCh38 chr16: 71,897,718-71,898,706 , GRCh37.p13 chr16: 71,931,621-71,932,609 IST1
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